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Downloaded from http://jme.bmj.com/ on February 1, 2018, Published by group.BMJ.research ethicsPAPERObtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents
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How to fill out obtaining informed consent for

01
Clearly explain the purpose and nature of the research or procedure to the participant.
02
Provide all necessary information about any potential risks or benefits involved.
03
Ensure that the participant has sufficient time to read and understand the consent form.
04
Allow the participant to ask any questions and address any concerns they may have.
05
Obtain the participant's signature or documented verbal consent.
06
Provide the participant with a copy of the signed consent form for their records.

Who needs obtaining informed consent for?

01
Researchers conducting medical experiments or clinical trials with human subjects.
02
Healthcare professionals obtaining consent for invasive procedures or surgeries.
03
Educational institutions conducting research involving students or faculty members.
04
Individuals conducting surveys or interviews that may involve personal or sensitive information.
05
Any person or entity performing research or experiments that require participant consent.
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Obtaining informed consent is to ensure that individuals understand the risks and benefits of participating in a study, procedure, or treatment before they agree to it.
Researchers, medical professionals, and organizations conducting studies or providing medical treatment are required to obtain informed consent.
Obtaining informed consent involves providing the necessary information to participants, allowing them to ask questions, and ensuring they have the capacity to make an informed decision before they sign the consent form.
The purpose of obtaining informed consent is to respect participants' autonomy and protect their rights by ensuring they understand the risks and benefits of their participation.
The information reported on obtaining informed consent forms typically includes details about the study or treatment, potential risks and benefits, confidentiality, voluntariness, and contact information for questions or concerns.
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